Katsura Yoshihiro, Kubota Hiroyuki, Kunida Katsuyuki, Kanno Akira, Kuroda Shinya, Ozawa Takeaki
Department of Chemistry, School of Science, The University of Tokyo, 7-3-1 Bunkyo-ku, Hongo, Tokyo 113-0033, Japan.
Department of Biological Sciences, School of Science, The University of Tokyo, 7-3-1 Bunkyo-ku, Hongo, Tokyo 113-0033, Japan.
Sci Rep. 2015 Oct 1;5:14589. doi: 10.1038/srep14589.
The dynamic activity of the serine/threonine kinase Akt is crucial for the regulation of diverse cellular functions, but the precise spatiotemporal control of its activity remains a critical issue. Herein, we present a photo-activatable Akt (PA-Akt) system based on a light-inducible protein interaction module of Arabidopsis thaliana cryptochrome2 (CRY2) and CIB1. Akt fused to CRY2phr, which is a minimal light sensitive domain of CRY2 (CRY2-Akt), is reversibly activated by light illumination in several minutes within a physiological dynamic range and specifically regulates downstream molecules and inducible biological functions. We have generated a computational model of CRY2-Akt activation that allows us to use PA-Akt to control the activity quantitatively. The system provides evidence that the temporal patterns of Akt activity are crucial for generating one of the downstream functions of the Akt-FoxO pathway; the expression of a key gene involved in muscle atrophy (Atrogin-1). The use of an optical module with computational modeling represents a general framework for interrogating the temporal dynamics of biomolecules by predictive manipulation of optogenetic modules.
丝氨酸/苏氨酸激酶Akt的动态活性对于多种细胞功能的调节至关重要,但其活性的精确时空控制仍然是一个关键问题。在此,我们基于拟南芥隐花色素2(CRY2)和CIB1的光诱导蛋白相互作用模块,提出了一种光激活Akt(PA-Akt)系统。与CRY2phr融合的Akt,CRY2phr是CRY2的最小光敏感结构域(CRY2-Akt),在生理动态范围内几分钟内通过光照可逆激活,并特异性调节下游分子和诱导性生物学功能。我们生成了CRY2-Akt激活的计算模型,使我们能够使用PA-Akt定量控制活性。该系统提供了证据,表明Akt活性的时间模式对于产生Akt-FoxO途径的下游功能之一;参与肌肉萎缩的关键基因(Atrogin-1)的表达至关重要。将光学模块与计算模型结合使用,代表了一个通过光遗传学模块的预测性操作来探究生物分子时间动态的通用框架。